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1. • Journal article

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   A new functional CYP3A4 intron 6 polymorphism significantly affects tacrolimus pharmacokinetics in kidney transplant recipients.

   Elens, Laure[UCL] Bouamar, Rachida Hesselink, Dennis A Haufroid, Vincent[UCL] van der Heiden, Ilse P van Gelder, Teun van Schaik, Ron H N (2011) Clinical Chemistry : international journal of molecular diagnostics and laboratory medicine — Vol. 57, no. 11, p. 1574-83 (2011)
2. • Journal article

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   The gene encoding rat 3-phosphoglycerate dehydrogenase.

   Robbi, Mariette[UCL] Achouri, Younes[UCL] Szpirer, C. Van Schaftingen, Emile[UCL] (2000) Mammalian genome : official journal of the International Mammalian Genome Society — Vol. 11, no. 11, p. 1034-6 (2000)
3. • Journal article

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   CYP3A4 intron 6 C>T SNP (CYP3A4*22) encodes lower CYP3A4 activity in cancer patients, as measured with probes midazolam and erythromycin.

   Elens, Laure[UCL] Nieuweboer, Annemieke Clarke, Stephen J Charles, Kellie A de Graan, Anne-Joy Haufroid, Vincent Mathijssen, Ron H J van Schaik, Ron H N (2013) Pharmacogenomics — Vol. 14, no.2, p. 137-149 (2013)
4. • Journal article

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   A vHNF1/TCF2-HNF6 cascade regulates the transcription factor network that controls generation of pancreatic precursor cells

   Poll, Aurélie V.[UCL] Pierreux, Christophe[UCL] Lokmane, Ludmilla Haumaitre, Cécile Achouri, Younes[UCL] Jacquemin, Patrick[UCL] Rousseau, Guy[UCL] Cereghini, Silvia Lemaigre, Frédéric[UCL] (2006) Diabetes — Vol. 55, no. 1, p. 61-69 (2006)
5. • Journal article

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   Suggestive evidence of associations between liver X receptor β polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT2 (Norway), MONICA (France) and HELENA (Europe)

   Solaas, Karianne Legry, Vanessa[UCL] Retterstol, Kjetil Berg, Paul R Holven, Kirsten B Ferrières, Jean Amouyel, Philippe Lien, Sigbjorn Romeo, Javier Valtueña, Jara Widhalm, Kurt Ruiz, Jonatan R Dallongeville, Jean Tonstad, Serena Rootwelt, Helge Halvorsen, Bente Nenseter, Marit S Birkeland, Kare I Thorsby, Per M Meirhaeghe, Aline Nebb, Hilde I (2010) BMC Medical Genetics — Vol. 11, p. 144 (2010)
6. • Journal article

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   Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretion

   Møller, A M Ek, J Durviaux, S M[UCL] Urhammer, SA Clausen, J O Eiberg, H Hansen, T Rousseau, Guy[UCL] Lemaigre, Frédéric[UCL] Pedersen, O (1999) Diabetologia : clinical and experimental diabetes and metabolism — Vol. 42, no. 8, p. 1011-1016 (1999)
7. • Journal article

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   Characterization of distinct mRNAs coding for putative isozymes of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.

   Crepin, K M Darville, M I Hue, Louis[UCL] Rousseau, Guy[UCL] (1989) European journal of biochemistry / FEBS — Vol. 183, no. 2, p. 433-40 (1989)
8. • Journal article

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   Approach to the molecular mechanisms of the modulation of growth hormone gene expression by glucocorticoid and thyroid hormones

   Rousseau, Guy[UCL] Eliard, P.H. Barlow, J.W. Lemaigre, Frédéric[UCL] Lafontaine, D.A. De Nayer, Philippe[UCL] Economidis, I. Formstecher, P. Idziorek, T. Mathy-Hartert, M. (1987) Journal of Steroid Biochemistry — Vol. 27, no. 1-3, p. 149-158 (1987)
9. • Journal article

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   The gene encoding disabled-1 (DAB1), the intracellular adaptor of the Reelin pathway, reveals unusual complexity in human and mouse.

   Bar, Isabelle Tissir, Fadel[UCL] Lambert de Rouvroit, Catherine De Backer, Olivier Goffinet, André[UCL] (2003) Journal of Biological Chemistry — Vol. 278, no.8, p. 5802-12 (2003)
10. • Journal article

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    5' flanking sequence and structure of a gene encoding rat 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.

    Darville, M I Crepin, K M Hue, Louis[UCL] Rousseau, Guy[UCL] (1989) Proceedings of the National Academy of Sciences of the United States of America — Vol. 86, no. 17, p. 6543-7 (1989)
11. • Journal article

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    Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A.

    Lannoy, Nathalie[UCL] Abinet, Isabelle[UCL] Bosmans, Arnaud[UCL] Lambert, Catherine[UCL] Vermylen, Christiane[UCL] Hermans, Cédric[UCL] (2012) Haemophilia : the official journal of the World Federation of Hemophilia — Vol. 18, no. 3, p. e331-e339 (2012)
12. • Journal article

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    Human peroxiredoxin 5 gene organization, initial characterization of its promoter and identification of alternative forms of mRNA.

    Nguyên-Nhu, Nhu Tiên Berck, Jehanne Clippe, André[UCL] Duconseille, Elee Cherif, Hanane Boone, Christophe Van der Eecken, Valérie[UCL] Bernard, Alfred[UCL] Banmeyer, Ingrid[UCL] Knoops, Bernard[UCL] (2007) Biochimica et biophysica acta — Vol. 1769, no. 7-8, p. 472-83 (2007)
13. • Journal article

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    ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants.

    Bauwens, Miriam Garanto, Alejandro Sangermano, Riccardo Naessens, Sarah Weisschuh, Nicole De Zaeytijd, Julie Khan, Mubeen Sadler, Françoise Balikova, Irina Van Cauwenbergh, Caroline Rosseel, Toon Bauwens, Jim De Leeneer, Kim De Jaegere, Sarah Van Laethem, Thalia De Vries, Meindert Carss, Keren Arno, Gavin Fakin, Ana Webster, Andrew R de Ravel de l'Argentière, Thomy J L Sznajer, Yves[UCL] Vuylsteke, Marnik Kohl, Susanne Wissinger, Bernd Cherry, Timothy Collin, Rob W J Cremers, Frans P M Leroy, Bart P De Baere, Elfride (2019) Genetics in medicine — Vol. 21, no.8, p. 1761-1771 (2019)
14. • Journal article

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    Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse.

    Vikkula, Miikka[UCL] Metsäranta, M Syvänen, A C Ala-Kokko, L Vuorio, E Peltonen, L (1992) The Biochemical journal — Vol. 285, no.Pt 1, p. 287-94 (1992)
15. • Journal article

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    Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility.

    Zhao, Jian Wu, Hui Khosravi, Melanie Cui, Huijuan Qian, Xiaoxia Kelly, Jennifer A Kaufman, Kenneth M Langefeld, Carl D Williams, Adrienne H Lauwerys, Bernard[UCL] (2011) PLoS Genetics — Vol. 7, no. 5, p. e1002079 (2011)
16. • Journal article

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    A gene expressed exclusively in acute B lymphoblastic leukemias.

    Vialle-Castellano, Alexandra Dupont, Sophie[UCL] Michaux, Lucienne[UCL] Laduron, Sandra De Plaen, Etienne[UCL] Jost, Edgar Ameye, Geneviève[UCL] Coulie, Pierre G.[UCL] Olive, Daniel Boon, Thierry[UCL] van Baren, Nicolas[UCL] (2004) Genomics — Vol. 83, no. 1, p. 85-94 (2004)
17. • Journal article

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    Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.

    Annunen, S Körkkö, J Czarny, M Warman, M L Brunner, H G Kääriäinen, H Mulliken, J B Tranebjaerg, L Brooks, D G Cox, G F Cruysberg, J R Curtis, M A Davenport, S L Friedrich, C A Kaitila, I. Krawczynski, M R Latos-Bielenska, A Mukai, S Olsen, B R Shinno, N Somer, M Vikkula, Miikka[UCL] Zlotogora, J Prockop, D J Ala-Kokko, L (1999) American journal of human genetics — Vol. 65, no. 4, p. 974-83 (1999)
18. • Journal article

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    Conjugative plasmid pAW63 brings new insights into the genesis of the Bacillus anthracis virulence plasmid pXO2 and of the Bacillus thuringiensis plasmid pBT9727.

    Van der Auwera, Géraldine[UCL] Andrup, Lars Mahillon, Jacques[UCL] (2005) BMC genomics — Vol. 6, p. 103 (2005)
19. • Journal article

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    An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.

    De Roeck, Arne Duchateau, Lena Van Dongen, Jasper Cacace, Rita Bjerke, Maria Van den Bossche, Tobi Cras, Patrick Vandenberghe, Rik De Deyn, Peter P Engelborghs, Sebastiaan Van Broeckhoven, Christine Sleegers, Kristel BELNEU Consortium Ivanoiu, Adrian[UCL] (2018) Acta neuropathologica — Vol. 135, no. 6, p. 827-837 (2018)
20. • Journal article

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    A single-stranded DNA binding protein required for mitochondrial DNA replication in S. cerevisiae is homologous to E. coli SSB.

    Van Dyck, E Foury, Françoise[UCL] Stillman, B. Brill, S J (1992) The EMBO journal — Vol. 11, no. 9, p. 3421-30 (1992)
21. • Journal article

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    Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive Nemaline myopathy

    Lehtokari, Vilma-Lotta Pelin, Katarina Sandbacka, Maria Ranta, Salla Donner, Kati Muntoni, Francesco Sewry, Caroline Angelini, Corrado Bushby, Kate Van den Bergh, Peter[UCL] Iannaccone, Susan Laing, Nigel G. Wallgren-Pettersson, Carina (2006) Human Mutation — Vol. 27, no. 9, p. 946-56 (2006)
22. • Journal article

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    Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant

    Ookawara, T Dave, V Willems, P. Martin, JJ. de Barsy, Thierry[UCL] Matthys, E Yoshida, A (1996) Archives of Biochemistry and Biophysics — Vol. 327, no. 1, p. 35-40 (1996)
23. • Journal article

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    Transcriptional analysis of the conjugative plasmid pAW63 from Bacillus thuringiensis.

    Van der Auwera, Géraldine Mahillon, Jacques[UCL] (2008) Plasmid — Vol. 60, no. 3, p. 190-199 (2008)
24. • Journal article

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    Hepatocyte nuclear factor 6: organization and chromosomal assignment of the rat gene and characterization of its promoter

    Rastegar, M Szpirer, C. Rousseau, Guy[UCL] Lemaigre, Frédéric[UCL] (1998) The Biochemical Journal — Vol. 334 ( Pt 3), p. 565-9 (1998)
25. • Journal article

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    Frequency of circulating Tregs with demethylated FOXP3 intron 1 in melanoma patients receiving tumor vaccines and potentially Treg-depleting agents.

    de Vries, I Jolanda M Castelli, Chiara Huygens, Caroline Jacobs, Joannes F M Stockis, Julie[UCL] Schuler-Thurner, Beatrice Adema, Gosse J Punt, Cornelis J A Rivoltini, Licia Schuler, Gerold Coulie, Pierre G.[UCL] Lucas, Sophie[UCL] (2011) Clinical Cancer Research — Vol. 17, no. 4, p. 841-8 (2011)

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